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MEISSA Adjustment Manual Patient Care Bed - Indonesia BPOM Medical Device Registration

MEISSA Adjustment Manual Patient Care Bed is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902123478. The device is manufactured by MEYSA TIBBI CIHAZLAR SAN. VE TIC. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MAIN MEDICAL PARTNERS.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : A
MEISSA Adjustment Manual Patient Care Bed
Analysis ID: AKL 10902123478

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Turkey

Authorized Representative

PT. MAIN MEDICAL PARTNERS

AR Address

JL. DR. Wahidin No 68 D,

Registration Date

Jun 15, 2021

Expiry Date

Nov 01, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Manual adjustable hospital bed.

Non Electromedic Non Sterile

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